NDC Code | 70518-1618-0 |
Package Description | 1 BLISTER PACK in 1 CARTON (70518-1618-0) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 70518-1618 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Pseudoephedrine Hydrochloride |
Non-Proprietary Name | Pseudoephedrine Hcl |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20191030 |
Marketing Category Name | ANDA |
Application Number | ANDA075153 |
Manufacturer | REMEDYREPACK INC. |
Substance Name | PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength | 120 |
Strength Unit | mg/1 |
Pharmacy Classes | Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC] |